Data / Medical devices / United States / Curio Digital Therapeutics
Curio Digital Therapeutics: FDA-registered device maker in Rocky Hill, NJ, United States, 1 510(k) clearance
Curio Digital Therapeutics is registered with the FDA (registration 3036503508) in Rocky Hill, NJ, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 22, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3036503508
- Address
- 10 Princeton Ave, Rocky Hill, NJ, United States, 08553
- Owner or operator
- Curio Digital Therapeutics (10092756)
- Roles
- Manufacturer
- First device listed
- February 14, 2025
- Registered through
- 2026
- Brand names listed
- MamaLift Plus
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Computerized Behavioral Therapy Device For Depressive Disorders. | SAP | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 22, 2024 | K223515 | MamaLift Plus | SAP | Substantially Equivalent | Curio Digital Therapeutics, Inc. | accessdata.fda.gov |
Compare with other makers
Updated April 22, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.